{{Rsnum
|rsid=1046896
|Gene=FN3KRP
|Chromosome=17
|position=82727657
|Orientation=plus
|GMAF=0.3861
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FN3KRP
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 49.6 | 38.1 | 12.4
| HCB | 21.2 | 53.3 | 25.5
| JPT | 23.9 | 52.2 | 23.9
| YRI | 61.2 | 33.3 | 5.4
| ASW | 47.4 | 43.9 | 8.8
| CHB | 21.2 | 53.3 | 25.5
| CHD | 26.6 | 57.8 | 15.6
| GIH | 30.7 | 55.4 | 13.9
| LWK | 53.6 | 38.2 | 8.2
| MEX | 31.0 | 53.4 | 15.5
| MKK | 53.2 | 39.7 | 7.1
| TSI | 33.3 | 54.9 | 11.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=20858683
|Title=Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways
|OA=1
}}

{{omim
|id=612940
|rsnum=1046896
}}

{{PMID Auto GWAS
  |PMID=24244560
  |Trait=Glycated hemoglobin levels
  |Title=A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry.
  |RiskAllele=T
  |Pval=2E-7
  |OR=.03
  |ORtxt=[0.019-0.043] unit increase
  }}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}